R Guerrini|E Andermann|M Avoli|W B Dobyns - JoVE Visualize

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Neurology|February 1, 1991

Epidermal nevus syndrome: a neurologic variant with hemimegalencephaly, gyral malformation, mental retardation, seizures, and facial hemihypertrophyL Pavone, P Curatolo, R Rizzo, et al.

Human Genetics|October 1, 1990

Rapid diagnosis of Miller-Dieker syndrome and isolated lissencephaly sequence by the polymerase chain reactionJ R Batanian, S A Ledbetter, R K Wolff, et al.

Nature|August 19, 1993

Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeatsO Reiner, R Carrozzo, Y Shen, et al.

The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|May 1, 1979

Oculomotor abnormalities in Friedreich's ataxiaT H Kirkham, D Guitton, A Katsarkas, et al.

Annals of Neurology|February 1, 1987

Anticonvulsants, folate levels, and pregnancy outcome: a prospective studyL V Dansky, E Andermann, D Rosenblatt, et al.

American Journal of Medical Genetics|July 9, 1999

Risk of abnormal pregnancy outcome in carriers of balanced reciprocal translocations involving the Miller-Dieker syndrome (MDS) critical region in chromosome 17p13.3T I Pollin, W B Dobyns, C A Crowe, et al.

American Journal of Human Genetics|November 1, 1988

Molecular detection of microscopic and submicroscopic deletions associated with Miller-Dieker syndromeP vanTuinen, W B Dobyns, D C Rich, et al.

Neuropediatrics|August 26, 1998

Microlissencephaly: a heterogeneous malformation of cortical developmentA J Barkovich, D M Ferriero, R M Barr, et al.

Neurology|October 24, 2001

Benign nocturnal alternating hemiplegia of childhood: six patients and long-term follow-upV Chaves-Vischer, F Picard, E Andermann, et al.

Birth Defects Original Article Series|January 1, 1975

Three familial midline malformtion syndromes of the central nervous system: agenesis of the corpus callosum and anterior horn-cell disease; agenesis of cerebellar vermis; and atrophy of the cerebellar vermisE Andermann, F Andermann, M Joubert, et al.

Pageof 64

Showing results (261-270 of 636) with videos related to

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Pageof 64

Neurology|February 1, 1991

Epidermal nevus syndrome: a neurologic variant with hemimegalencephaly, gyral malformation, mental retardation, seizures, and facial hemihypertrophyL Pavone, P Curatolo, R Rizzo, et al.

Human Genetics|October 1, 1990

Rapid diagnosis of Miller-Dieker syndrome and isolated lissencephaly sequence by the polymerase chain reactionJ R Batanian, S A Ledbetter, R K Wolff, et al.

Nature|August 19, 1993

Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeatsO Reiner, R Carrozzo, Y Shen, et al.

The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|May 1, 1979

Oculomotor abnormalities in Friedreich's ataxiaT H Kirkham, D Guitton, A Katsarkas, et al.

Annals of Neurology|February 1, 1987

Anticonvulsants, folate levels, and pregnancy outcome: a prospective studyL V Dansky, E Andermann, D Rosenblatt, et al.

American Journal of Medical Genetics|July 9, 1999

Risk of abnormal pregnancy outcome in carriers of balanced reciprocal translocations involving the Miller-Dieker syndrome (MDS) critical region in chromosome 17p13.3T I Pollin, W B Dobyns, C A Crowe, et al.

American Journal of Human Genetics|November 1, 1988

Molecular detection of microscopic and submicroscopic deletions associated with Miller-Dieker syndromeP vanTuinen, W B Dobyns, D C Rich, et al.

Neuropediatrics|August 26, 1998

Microlissencephaly: a heterogeneous malformation of cortical developmentA J Barkovich, D M Ferriero, R M Barr, et al.

Neurology|October 24, 2001

Benign nocturnal alternating hemiplegia of childhood: six patients and long-term follow-upV Chaves-Vischer, F Picard, E Andermann, et al.

Birth Defects Original Article Series|January 1, 1975

Three familial midline malformtion syndromes of the central nervous system: agenesis of the corpus callosum and anterior horn-cell disease; agenesis of cerebellar vermis; and atrophy of the cerebellar vermisE Andermann, F Andermann, M Joubert, et al.

Pageof 64